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  5. Design and Synthesis of Novel Tylophorine Analogs and their Biological Activity
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Design and Synthesis of Novel Tylophorine Analogs and their Biological Activity

Date Issued
December 1, 2009
Author(s)
Gutierrez, Julio
Advisor(s)
David C. Baker
Additional Advisor(s)
Michael D. Best
Ziling (Ben) Xue
Engin H. Serpersu
Permanent URI
https://trace.tennessee.edu/handle/20.500.14382/27300
Abstract

Alkaloids containing the nitrogen atom in the bridgehead position of two rings, such as indolizidine, pyrrolizidine, and quinolizidine alkaloids, have a wide and varied distribution in nature. Some of these alkaloids demonstrate a broad range of pharmacological activities and have generated substantial synthetic interest. This thesis covers the total synthesis of novel tylophorine analogs called DCB 3503, DCB 3506, DCB 3507, DCB 3508, DCB 3509, and a derivative with a biotinylated chain attached to DCB 3506 for use as a biological probe. This thesis discusses the biological activity of these compounds as well.

Disciplines
Chemistry
Degree
Doctor of Philosophy
Major
Chemistry
Embargo Date
December 1, 2011
File(s)
Thumbnail Image
Name

GutierrezJulio.pdf

Size

36.29 MB

Format

Adobe PDF

Checksum (MD5)

56a768eceaab45939da6ab8dad3717a0


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